Colorectal cancer risk in patients with inflammatory bowel disease and Lynch syndrome

por Aronson, Melyssa, Stempak, Joanne, Silverberg, Mark, Semotiuk, Kara, Gryfe, Robert, Gallinger, Steven
Publicado 2010

Patient-physician relationships, health self-efficacy, and gynecologic cancer screening among women with Lynch syndrome

por McGarragle, Kaitlin M., Aronson, Melyssa, Semotiuk, Kara, Holter, Spring, Hare, Crystal J., Ferguson, Sarah E., Cohen, Zane, Hart, Tae L.
Publicado 2019

Desmoid Tumors in Familial Adenomatous Polyposis Patients: Favorable Outcomes with Multidisciplinary Management

por Al-Sukhni, Eisar, Shapiro, Joel, Suraweera, Harini, Semotiuk, Kara, Swallow, Carol J., Brar, Savtaj, Razak, Albiruni, Gupta, Abha A., Gladdy, Rebecca A.
Publicado 2023

Clinicopathologic and genetic features of young patients with colorectal cancer

por Aronson, Melyssa, Gallinger, Steve, Rothenmund, Heidi, Semotiuk, Kara, Holter, Spring, Berk, Terri, Pollett, Aaron, Cohen, Zane, Bapat, Bharati, Kim, Hyeja, Gryfe, Robert
Publicado 2010

Hereditary colorectal cancer screening: A 10-year longitudinal cohort study following an educational intervention

por Carroll, June C., Permaul, Joanne A., Semotiuk, Kara, Yung, Eric M., Blaine, Sean, Dicks, Elizabeth, Warner, Ellen, Rothenmund, Heidi, Esplen, Mary Jane, Moineddin, Rahim, McLaughlin, John
Publicado 2020

Incidental findings from cancer next generation sequencing panels

por Maani, Nika, Panabaker, Karen, McCuaig, Jeanna M., Buckley, Kathleen, Semotiuk, Kara, Farncombe, Kirsten M., Ainsworth, Peter, Panchal, Seema, Sadikovic, Bekim, Armel, Susan Randall, Lin, Hanxin, Kim, Raymond H.
Publicado 2021

Development and validation of a brief screening instrument for psychosocial risk associated with genetic testing: a pan-Canadian cohort study

por Esplen, Mary Jane, Cappelli, Mario, Wong, Jiahui, Bottorff, Joan L, Hunter, Jon, Carroll, June, Dorval, Michel, Wilson, Brenda, Allanson, Judith, Semotiuk, Kara, Aronson, Melyssa, Bordeleau, Louise, Charlemagne, Nicole, Meschino, Wendy
Publicado 2013

Quality of life drives patients’ preferences for secondary findings from genomic sequencing

por Mighton, Chloe, Carlsson, Lindsay, Clausen, Marc, Casalino, Selina, Shickh, Salma, McCuaig, Laura, Joshi, Esha, Panchal, Seema, Semotiuk, Kara, Ott, Karen, Elser, Christine, Eisen, Andrea, Kim, Raymond H., Lerner-Ellis, Jordan, Carroll, June C., Glogowski, Emily, Schrader, Kasmintan, Bombard, Yvonne
Publicado 2020

Additional germline findings from a tumor profiling program

por Stjepanovic, Neda, Stockley, Tracy L., Bedard, Philippe L., McCuaig, Jeanna M., Aronson, Melyssa, Holter, Spring, Semotiuk, Kara, Leighl, Natasha B., Jang, Raymond, Krzyzanowska, Monika K., Oza, Amit M., Gupta, Abha, Elser, Christine, Ahmed, Lailah, Wang, Lisa, Kamel-Reid, Suzanne, Siu, Lillian L., Kim, Raymond H.
Publicado 2018

Evaluation of a decision aid for incidental genomic results, the Genomics ADvISER: protocol for a mixed methods randomised controlled trial

por Shickh, Salma, Clausen, Marc, Mighton, Chloe, Casalino, Selina, Joshi, Esha, Glogowski, Emily, Schrader, Kasmintan A, Scheer, Adena, Elser, Christine, Panchal, Seema, Eisen, Andrea, Graham, Tracy, Aronson, Melyssa, Semotiuk, Kara M, Winter-Paquette, Laura, Evans, Michael, Lerner-Ellis, Jordan, Carroll, June C, Hamilton, Jada G, Offit, Kenneth, Robson, Mark, Thorpe, Kevin E, Laupacis, Andreas, Bombard, Yvonne
Publicado 2018